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34343

Supelco

Fenoxycarb

PESTANAL®, analytical standard

Sinonimo/i:

Ethyl 2-(4-phenoxyphenoxy)ethylcarbamate

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About This Item

Formula empirica (notazione di Hill):
C17H19NO4
Numero CAS:
72490-01-8
Peso molecolare:
301.34
Beilstein:
6932817
Numero CE:
276-696-7
Numero MDL:
MFCD00144303
Codice UNSPSC:
41116107
ID PubChem:
329754956
NACRES:
NA.24
Prezzi e disponibilità al momento non sono disponibili

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

CCOC(=O)NCCOc1ccc(Oc2ccccc2)cc1

InChI

1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19)
HJUFTIJOISQSKQ-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Fenoxycarb is a neurotoxic carbamate[1][2], insect growth regulator[1] or public health insecticide[2], which can exhibit potent insect juvenile hormone-mimic activity, which causes disturbance in the development, reproduction and behaviour of insects[2]. It can be used to control a wide variety of insect pests[1], basically in agriculture, forestry, and stored products.[2]

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Note legali

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Health hazardEnvironment
GHS08,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H351,H410

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCK5935
BCCG3127
BCBT7968

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Sexually dimorphic traits are common and widespread among animals. The expression of the Doublesex-/Mab-3-domain (DM-domain) gene family has been widely studied in model organisms and has been proven to be essential for the development and maintenance of sex-specific traits. However
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Male moths use sex pheromones to find their mating partners. In the moth, Agrotis ipsilon, the behavioral response and the neuron sensitivity within the primary olfactory centre, the antennal lobe (AL), to sex pheromone increase with age and juvenile hormone
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Insect molecular biology, 19(1), 77-86 (2009-12-17)
Sex pheromone production in Helicoverpa armigera is regulated by pheromone-biosynthesis-activating neuropeptide (PBAN), which binds to a G-protein coupled receptor at the pheromone gland. We demonstrate the temporal differential expression levels of the PBAN receptor (PBAN-R) gene, reaching peak levels at
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It was reported that males daphnid Daphnia magna that have been induced by methyl farnesoate exposure exhibit higher tolerance to chemical compounds such as potassium dichromate and pentachlorophenol than females. Male neonates are also known to be induced by exposure
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